Genetic identification and molecular modeling characterization of a novel POU3F4 variant in two Italian deaf brothers.

Giannantonio, Sara

Genetic identification and molecular modeling characterization of a novel POU3F4 variant in two Italian deaf brothers. [electronic resource] - International journal of pediatric otorhinolaryngology Feb 2020 - 109790 p. digital

Publication Type: Case Reports; Journal Article

1872-8464

10.1016/j.ijporl.2019.109790 doi


Child, Preschool
Deafness--genetics
Female
Genetic Diseases, X-Linked--genetics
Hearing Loss, Conductive--genetics
Hearing Loss, Sensorineural--genetics
Humans
Infant
Italy
Male
Models, Molecular
Mutation, Missense
POU Domain Factors--chemistry
Pedigree
Protein Folding
Siblings